chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	160425853	160425854	A	G	13	GENIC	heterozygous	56359399
5	160426593	160426594	T	C	15	GENIC	homozygous	56359401
5	160426918	160426919	A	G	31	GENIC	possibly homozygous	56359403
5	160427454	160427455	G	A	10	GENIC	homozygous	56359405
5	160428235	160428236	T	C	17	GENIC	possibly homozygous	56359407
5	160429442	160429443	C	T	11	GENIC	possibly homozygous	56359409
5	160429840	160429841	G	T	13	GENIC	homozygous	56359411
5	160430585	160430586	A	G	13	GENIC	possibly homozygous	56359413
5	160431253	160431254	C	T	24	GENIC	homozygous	56359415
5	160431991	160431992	T	C	28	GENIC	possibly homozygous	56359417
5	160432581	160432582	T	C	15	GENIC	homozygous	56359419
5	160433205	160433206	G	GC	20	GENIC	homozygous	56359421
5	160433988	160433989	A	ATGTGTGTG	1	GENIC	homozygous	56359423
5	160434508	160434509	A	ATG	3	GENIC	homozygous	56359424
5	160435164	160435165	G	A	20	GENIC	possibly homozygous	56359426
5	160435417	160435418	A	C	14	GENIC	possibly homozygous	56359428
5	160436002	160436003	C	T	11	GENIC	homozygous	56359430